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3-[6-(hydroxyamino)-9H-purin-9-yl]propane-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85446-34-0

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85446-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85446-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,4 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85446-34:
(7*8)+(6*5)+(5*4)+(4*4)+(3*6)+(2*3)+(1*4)=150
150 % 10 = 0
So 85446-34-0 is a valid CAS Registry Number.

85446-34-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[6-(hydroxyamino)purin-9-yl]propane-1,2-diol

1.2 Other means of identification

Product number -
Other names 6-hydroxylamino-9-(2,3-dihydroxypropyl)purine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:85446-34-0 SDS

85446-34-0Downstream Products

85446-34-0Relevant academic research and scientific papers

SYNTHESIS OF (3-HYDROXY-2-PHOSPHONYLMETHOXYPROPYL) DERIVATIVES OF HETEROCYCLIC BASES

Holy, Antonin,Rosenberg, Ivan,Dvorakova, Hana

, p. 2470 - 2501 (2007/10/02)

Analogs of antiviral 9-(S)-(3-hydroxy-2-phosphonylmethoxypropyl)adenine (HPMPA, I), containing modofied heterocyclic base, were prepared from racemic or (S)-N-(2,3-dihydroxypropyl) derivatives II.Compounds II are heated with chloromethylphosphonyl dichlor

Synthesis of aliphatic nucleoside analogues with potential antiviral activity

Colla,Busson,De Clercq,Vanderhaeghe

, p. 569 - 576 (2007/10/02)

The synthesis of a series of double-modified adenosine and 8-aza-adenosine analogues, altered in the 6-position of the base and having the sugar moiety replaced by an acyclic hydroxylated side chain is described. Also, some aliphatic derivatives of 5-iodo- and E-5-(2-bromovinyl)uracil were prepared. Of all these compounds, only 6-hydroxylamino-9-(2,3-dihydroxypropyl)purine displayed some antiviral activity when tested in primary rabbit kidney cell cultures against vesicular stomatitis, vaccinia or herpes simplex virus.

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